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Gene entry

FANCI

FA complementation group I

Chromosome
15
Cytoband
15q26.1
Variants (rsID)
37

FANCI is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q26.1). Its official name is “FA complementation group I”. The reference table lists 37 variants (rsID) for this gene.

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Clinically classified variants

25 reference-table entries with clinical significance.

  • rs114549781Benignsingle nucleotide variantFanconi anemia
  • rs115048121Benignsingle nucleotide variantFanconi anemia complementation group I|Progressive sclerosing poliodystrophy
  • rs117125761Benignsingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia|Fanconi anemia complementation group I
  • rs118031800Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs138675752Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs139814895Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs149243307Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs2307441Benignsingle nucleotide variantMitochondrial disease|Fanconi anemia|Progressive sclerosing poliodystrophy|6 conditions|Seizure|Association with valproate-induced liver toxicity|POLG-Related Spectrum Disorders|Hereditary spastic paraplegia
  • rs3087374Benignsingle nucleotide variantFanconi anemia|POLG-Related Spectrum Disorders|Seizure|Progressive sclerosing poliodystrophy|Fanconi anemia complementation group I|Hereditary spastic paraplegia
  • rs34405660Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs62020347Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs79685648Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs144908351Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs145349375Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs149008055Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs151169233Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs191202700Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs536522307Conflicting interpretationssingle nucleotide variantFanconi anemia|Progressive sclerosing poliodystrophy|Fanconi anemia complementation group I
  • rs864622739Likely pathogenicsingle nucleotide variantFanconi anemia
  • rs375656231Pathogenicsingle nucleotide variantFanconi anemia complementation group I|Fanconi anemia
  • rs139181400Uncertain significancesingle nucleotide variantFanconi anemia
  • rs142969866Uncertain significancesingle nucleotide variantFanconi anemia
  • rs182154506Uncertain significancesingle nucleotide variantFanconi anemia|Fanconi anemia complementation group I
  • rs200007225Uncertain significancesingle nucleotide variantFanconi anemia
  • rs201553891Uncertain significancesingle nucleotide variantFanconi anemia

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.